Abstract
The practical use of Zn metal anodes in aqueous zinc batteries is impeded by the growth of dendrites, anode corrosion, and hydrogen evolution reaction in aqueous electrolytes. In this study, a simple, energy-efficient, and scalable approach is reported to mitigate these detrimental issues effectively. Using 1-hexanethiol (HT), a hydrophobic self-assembled mercaptan layer (SAML) with a highly ordered structure is in situ created on the surface of the Zn anode. This ultrathin interfacial structure guides uniform Zn deposition and shields the Zn anode from water and oxygen-induced corrosion, thus effectively inhibiting dendrite formation and side reactions. Consequently, the HT-Zn electrode showcases impressive electrochemical stability and reversibility, and the as-assembled HT-Zn||I2 full cell delivers increased specific capacity (from 112 to 155 mAh g−1 at 1 A g−1) and ultra-stable cyclability (zero capacity decay during the extended 1500 cycles at 4 A g−1). To validate the effectiveness of this simple and scalable method, a large-sized pouch cell is prepared, which can be stably operated for 1000 cycles with a capacity decay of merely 0.0098% per cycle and Coulombic efficiency exceeding 99.1%. The presented SAML strategy highlights the potential of molecular engineering in improving the performance of aqueous zinc batteries. © 2023 Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | 2302970 |
| Journal | Advanced Energy Materials |
| Volume | 14 |
| Issue number | 3 |
| Online published | 30 Nov 2023 |
| DOIs | |
| Publication status | Published - 19 Jan 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Research Keywords
- anode corrosion
- aqueous batteries
- zinc anode
- zinc batteries
- zinc dendrites
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